Gordeeva Alina E, Sharapov Mars G, Tikhonova Irina V, Chemeris Nikolay K, Fesenko Evgeniy E, Novoselov Vladimir I, Temnov Andrey A
Institute of Cell Biophysics, Russian Academy of Sciences, Pushchino, Russia.
Cells Tissues Organs. 2017;203(6):353-364. doi: 10.1159/000455830. Epub 2017 Mar 9.
Ischemia/reperfusion (I/R) injury of the small intestine caused by occlusion of the superior mesenteric artery affects the intestinal tissue as well as components of the blood circulatory system from the microvasculature to mesenteric vessels. The aim of this work was to study the correlation between the dynamics of destruction development in the intestinal tissue, microvasculature, and mesenteric vessels in I/R of the small intestine. The microvasculature was analyzed by whole-organ continuous monitoring of the intestinal mucosal blood perfusion by laser Doppler flowmetry during the entire I/R. Real-time RT-PCR was used to assess gene expression of NF-κB, caspase-3, Ki67, and TNF-α in blood vessels. At the start of reperfusion, the first targets to be disrupted are microvessels in the apical villi. Injury of the apical part of the microcirculatory bloodstream correlates with the reduction in intestinal mucosal blood perfusion, which occurred simultaneously with apical villous destruction. By the end of the reperfusion period, the low intestinal mucosal blood perfusion is mirrored by the destruction of the microvasculature and mucosal structures in the entire organ. The development of mesenteric vessel injury is characterized by a change in NO metabolism and damaged endothelial cells concomitant with an alteration in the expression of genes encoding NF-κB, caspase-3, and Ki67 by the end of the reperfusion period. In I/R injury, detrimental effects on the intestinal tissue, microvasculature, and mesenteric vessels develop and exhibit common mechanisms of function, which show strong correlations.
肠系膜上动脉闭塞引起的小肠缺血/再灌注(I/R)损伤会影响肠组织以及从微血管到肠系膜血管的血液循环系统的组成部分。这项工作的目的是研究小肠I/R过程中肠组织、微血管和肠系膜血管中破坏发展动态之间的相关性。在整个I/R过程中,通过激光多普勒血流仪对肠黏膜血流灌注进行全器官连续监测来分析微血管。实时逆转录聚合酶链反应用于评估血管中NF-κB、半胱天冬酶-3、Ki67和肿瘤坏死因子-α的基因表达。在再灌注开始时,首先受到破坏的靶点是顶端绒毛中的微血管。微循环血流顶端部分的损伤与肠黏膜血流灌注的减少相关,这与顶端绒毛破坏同时发生。到再灌注期结束时,整个器官中微血管和黏膜结构的破坏反映出肠黏膜血流灌注较低。肠系膜血管损伤的发展特征是一氧化氮代谢改变和内皮细胞受损,同时在再灌注期结束时,编码NF-κB、半胱天冬酶-3和Ki67的基因表达也发生改变。在I/R损伤中,对肠组织、微血管和肠系膜血管的有害影响会发展并表现出共同的功能机制,这些机制显示出很强的相关性。